ACME United Corporation Recalls Savannah Antibacterial Towelettes Due to CGMP Deviations

What Happened

ACME United Corporation, based in Shelton, CT, has initiated a voluntary recall of Savannah Antibacterial Towelettes. The recall, which has been classified as Class II by the FDA, was prompted by Current Good Manufacturing Practice (CGMP) deviations. The firm began the notification process via letter on January 20, 2026.

Which Products Are Affected

The recall affects Savannah Antibacterial Towelettes (Benzalkonium Chloride 0.13%), packaged as individual 4 x 7 towelettes. The products are labeled under R&R Enterprise with NDC 59647-749-02. The following lot numbers and expiration dates are included in this recall:

• Lot #: MN24623, Exp. Date Jul 2028
• Lot #: MN27023, Exp. Date Aug 2028
• Lot #: MN32423, Exp. Date Oct 2028
• Lot #: MN300724, Exp. Date Dec 2028

These products were distributed nationwide within the United States.

What You Should Do

Consumers and distributors who have these specific lots of Savannah Antibacterial Towelettes in their possession should identify the affected products by checking the lot numbers and expiration dates on the packaging. While the source data does not specify a return process, consumers typically should stop using recalled medical products and contact the recalling firm, ACME United Corporation, for further instructions regarding disposal or returns.

Why This Matters

This recall is significant because CGMP deviations indicate that the product may not have been manufactured under the strict quality and safety standards required for drug products. A Class II classification suggests that use of the product may cause temporary or medically reversible adverse health consequences.

Source

This information is provided by the FDA under recall number D-0364-2026.